Holocarboxylase synthetase deficiency (Q5883885)

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Human disease
  • Biotin-(propionyl-CoA-carboxylase) ligase deficiency (disorder)
  • Multiple carboxylase deficiency - neonatal onset (disorder)
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Language Label Description Also known as
English
Holocarboxylase synthetase deficiency
Human disease
  • Biotin-(propionyl-CoA-carboxylase) ligase deficiency (disorder)
  • Multiple carboxylase deficiency - neonatal onset (disorder)

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